A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2969265



Internal ID15435695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112620947..112823547hg38UCSC Ensembl
Innerchr9:115383227..115585827hg19UCSC Ensembl
Innerchr9:114423048..114625648hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38202601
hg19202601
hg18202601
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515121
Supporting Variants
SamplesNA21366
Known GenesINIP, KIAA1958, SNX30
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2969265
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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